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Search results (501)

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Microperimetry as an Outcome Measure Improves Patient Eligibility and Efficacy Detection in RPGR Gene Therapy Trials

JOSAN AS. et al, (2026), American Journal of Ophthalmology, 290, 61 - 69

Centripetal Retinal Degeneration Follows an Exponential Decay and May Be Reversed Following Gene Therapy

ABDALLA  ELSAYED MEA. et al, (2026), American Journal of Ophthalmology, 289, 76 - 86

Quantification of Ocular Gene Therapy–Related Inflammation Using the VRMACS Grading System

Abdalla Elsayed MEA. and MacLaren RE., (2026), Ophthalmology Science, 6

CDHR1-associated retinal degeneration: Clinical phenotypes and therapeutic approaches.

Narayan AR. et al, (2026), Prog Retin Eye Res, 114

Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy

Abdalla Elsayed MEA. et al, (2026), Investigative Ophthalmology Visual Science, 67

Interactions Between Epidermal Growth Factor-Containing Fibulin-Like Extracellular Matrix Protein 1 and Tissue Inhibitor of Metalloproteinases-3 and Relevance to Age-Related Macular Degeneration.

Ehrenzeller C. and MacLaren RE., (2026), Ophthalmol Sci, 6

Macular holes in inherited retinal dystrophies and vitreoretinopathies.

Abdalla Elsayed MEA. et al, (2026), Surv Ophthalmol

Clinical Spectrum and Genetics of Ocular Manifestations in Muscle Eye Brain Disease: A Literature Review.

Christou EE. et al, (2026), Semin Ophthalmol, 1 - 8

Genotypic and Phenotypic Insights on 11 Novel Variants in the ABCA4 Gene.

Al-Khuzaei S. et al, (2026), Genes (Basel), 17

Letter to the Editor Regarding "Multiwavelength Photobiomodulation Improves Multiple Aspects of Visual Function in Early-Stage Dry Age-Related Macular Degeneration".

Karakosta C. and MacLaren RE., (2026), Ophthalmol Ther, 15, 2095 - 2097

Exploring fundus-controlled mesopic and scotopic perimetry in inherited retinal disease.

Taylor LJ. et al, (2026), Acta Ophthalmol

Geographic atrophy in age-related macular degeneration: phenotypic characterisation for clinical trial consideration.

Borchert GA. et al, (2026), Graefes Arch Clin Exp Ophthalmol, 264, 1201 - 1216

Ophthalmic manifestations of mitochondrial disorders.

Baxter MF. et al, (2026), Prog Retin Eye Res, 112

IMPG2-associated retinal dystrophy with a novel missense variant and therapeutic options via adenine base editing.

Abdalla Elsayed MEA. et al, (2026), Ophthalmic Genet, 47, 172 - 178

A novel EYS c.6192-1G>A variant presents ideal base editing therapeutic opportunities.

Kaukonen M. et al, (2026), Ophthalmic Genet, 47, 195 - 198

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